L. Shao

Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.

Z. Ou, P. Stankiewicz, Z. Xia, 2011, Genome research.

A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles.

L. Shao, D. del Gaudio, I. B. Van den Veyver, 2008, Molecular human reproduction.

ERG amplification is a secondary recurrent driver event in myeloid malignancy with complex karyotype and TP53 mutations

L. Shao, D. Bixby, Hong Xiao, 2022, Genes, chromosomes & cancer.

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases

P. Stankiewicz, L. Shao, Ankita Patel, 2008, American journal of medical genetics. Part A.

Array comparative genomic hybridization detects chromosomal abnormalities in hematological cancers that are not detected by conventional cytogenetics.

L. Shao, Ankita Patel, C. Shaw, 2010, The Journal of molecular diagnostics : JMD.

Low‐level mosaicism of trisomy 14: Phenotypic and molecular characterization

L. Shao, Ankita Patel, C. Shaw, 2008, American journal of medical genetics. Part A.